L Weiss, W A Reynolds. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Abnormalities, Multiple/geneticsBone and Bones/abnormalitiesChild, PreschoolChromosome AberrationsChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 4-5Clavicle/abnormalitiesCri-du-Chat SyndromeDown SyndromeFemaleFingers/abnormalitiesHumansInfantInfant, NewbornKaryotypingKlinefelter SyndromeMaleMetacarpus/abnormalitiesMetatarsus/abnormalitiesPelvic Bones/abnormalitiesToes/abnormalitiesTrisomyTurner Syndrome
Year: 1972 PMID： 4264453
Source DB: PubMed Journal: Orthop Clin North Am ISSN： 0030-5898 Impact factor: 2.472